In Hospital 24 Hour Observation of Syncope Patients
Recruiting
Observational Study
Syncope
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Observational
- Participants needed
- 640 (estimated)
- Sponsor
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Other
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About This Trial
Syncope is very common and has a broad differential diagnosis. Guidelines on syncope recommend to apply guideline based syncope algorithm (SA) to identify low- / intermediate risk syncope patients and recommend to discharge these patients. The time window when to discharge these patients is not defined in the guidelines. In current medical practice low- / intermediate risk syncope patients are eit…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
All patients that are assessed as low- and intermediate risk syncope, are eligible for inclusion in this trial.
The initial syncope evaluation includes:
1. Complete and thorough history taking of the syncope event and past medical history
2. Physical examination including supi…
Contacts